TY - JOUR
T1 - Association of traumatic brain injury with subsequent neurological and psychiatric disease
T2 - A meta-analysis
AU - Perry, David C.
AU - Sturm, Virginia E.
AU - Peterson, Matthew J.
AU - Pieper, Carl F.
AU - Bullock, Thomas
AU - Boeve, Bradley F.
AU - Miller, Bruce L.
AU - Guskiewicz, Kevin M.
AU - Berger, Mitchel S.
AU - Kramer, Joel H.
AU - Welsh-Bohmer, Kathleen A.
N1 - Funding Information:
Dr. Sturm is supported by National Institute on Aging 1K23AG040127. Dr. Peterson is supported by National Cancer Institute Award KM1CA156687. Dr. Boeve receives research support from the National Institute on Aging (P50 AG016574, U01 AG006786, R01 AG032306, and R01 AG041797) and the Mangurian Foundation. Dr. Miller is funded by NIH grants P50AG023501, P01AG019724, P50 AG1657303, and the state of California. Dr. Welsh-Bohmer received funding from the National Institute of Aging (P30 AG28377) and from private donors to the Joseph & Kathleen Bryan Alzheimer’s Disease Center at Duke University.
Publisher Copyright:
©AANS, 2016.
PY - 2016
Y1 - 2016
N2 - OBJECTIVE: Mild traumatic brain injury (TBI) has been proposed as a risk factor for the development of Alzheimer’s disease, Parkinson’s disease, depression, and other illnesses. This study’s objective was to determine the association of prior mild TBI with the subsequent diagnosis (that is, at least 1 year postinjury) of neurological or psychiatric disease. METHODS: All studies from January 1995 to February 2012 reporting TBI as a risk factor for diagnoses of interest were identified by searching PubMed, study references, and review articles. Reviewers abstracted the data and assessed study designs and characteristics. RESULTS: Fifty-seven studies met the inclusion criteria. A random effects meta-analysis revealed a significant association of prior TBI with subsequent neurological and psychiatric diagnoses. The pooled odds ratio (OR) for the development of any illness subsequent to prior TBI was 1.67 (95% CI 1.44–1.93, p < 0.0001). Prior TBI was independently associated with both neurological (OR 1.55, 95% CI 1.31–1.83, p < 0.0001) and psychiatric (OR 2.00, 95% CI 1.50–2.66, p < 0.0001) outcomes. Analyses of individual diagnoses revealed higher odds of Alzheimer’s disease, Parkinson’s disease, mild cognitive impairment, depression, mixed affective disorders, and bipolar disorder in individuals with previous TBI as compared to those without TBI. This association was present when examining only studies of mild TBI and when considering the influence of study design and characteristics. Analysis of a subset of studies demonstrated no evidence that multiple TBIs were associated with higher odds of disease than a single TBI. CONCLUSIONS: History of TBI, including mild TBI, is associated with the development of neurological and psychiatric illness. This finding indicates that either TBI is a risk factor for heterogeneous pathological processes or that TBI may contribute to a common pathological mechanism.
AB - OBJECTIVE: Mild traumatic brain injury (TBI) has been proposed as a risk factor for the development of Alzheimer’s disease, Parkinson’s disease, depression, and other illnesses. This study’s objective was to determine the association of prior mild TBI with the subsequent diagnosis (that is, at least 1 year postinjury) of neurological or psychiatric disease. METHODS: All studies from January 1995 to February 2012 reporting TBI as a risk factor for diagnoses of interest were identified by searching PubMed, study references, and review articles. Reviewers abstracted the data and assessed study designs and characteristics. RESULTS: Fifty-seven studies met the inclusion criteria. A random effects meta-analysis revealed a significant association of prior TBI with subsequent neurological and psychiatric diagnoses. The pooled odds ratio (OR) for the development of any illness subsequent to prior TBI was 1.67 (95% CI 1.44–1.93, p < 0.0001). Prior TBI was independently associated with both neurological (OR 1.55, 95% CI 1.31–1.83, p < 0.0001) and psychiatric (OR 2.00, 95% CI 1.50–2.66, p < 0.0001) outcomes. Analyses of individual diagnoses revealed higher odds of Alzheimer’s disease, Parkinson’s disease, mild cognitive impairment, depression, mixed affective disorders, and bipolar disorder in individuals with previous TBI as compared to those without TBI. This association was present when examining only studies of mild TBI and when considering the influence of study design and characteristics. Analysis of a subset of studies demonstrated no evidence that multiple TBIs were associated with higher odds of disease than a single TBI. CONCLUSIONS: History of TBI, including mild TBI, is associated with the development of neurological and psychiatric illness. This finding indicates that either TBI is a risk factor for heterogeneous pathological processes or that TBI may contribute to a common pathological mechanism.
KW - Dementia
KW - Head injury
KW - Meta-analysis
KW - Psychiatry
KW - Traumatic brain injury
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U2 - 10.3171/2015.2.JNS14503
DO - 10.3171/2015.2.JNS14503
M3 - Review article
C2 - 26315003
AN - SCOPUS:85017011274
SN - 0022-3085
VL - 124
SP - 511
EP - 526
JO - Journal of Neurosurgery
JF - Journal of Neurosurgery
IS - 2
ER -